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Nature Genetics|June 1, 1992
Peripheral myelin protein-22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot-Marie-Tooth 1AN Matsunami, B Smith, L Ballard, et al.Nature Genetics|June 1, 1992
Characterization of a yeast artificial chromosome contig spanning the Huntington's disease gene candidate regionG P Bates, J Valdes, H Hummerich, et al.Nature Genetics|June 1, 1992
Evidence for at least four Fanconi anaemia genes including FACC on chromosome 9C A Strathdee, A M Duncan, M BuchwaldNature Genetics|June 1, 1992
Isolation of a candidate gene for Norrie disease by positional cloningW Berger, A Meindl, T J van de Pol, et al.Nature Genetics|June 1, 1992
A null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosaP J Rosenfeld, G S Cowley, T L McGee, et al.Nature Genetics|June 1, 1992
Presenile dementia and cerebral haemorrhage linked to a mutation at codon 692 of the beta-amyloid precursor protein geneL Hendriks, C M van Duijn, P Cras, et al.Nature Genetics|October 1, 1992
Human homologs of a Drosophila Enhancer of split gene product define a novel family of nuclear proteinsS Stifani, C M Blaumueller, N J Redhead, et al.Nature Genetics|October 1, 1992
A germline mutation in the androgen receptor gene in two brothers with breast cancer and Reifenstein syndromeR Wooster, J Mangion, R Eeles, et al.Nature Genetics|October 1, 1992
Missense glucokinase mutation in maturity-onset diabetes of the young and mutation screening in late-onset diabetesM Stoffel, P Patel, Y M Lo, et al.Pageof 744